Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 115879573 | 11587957 | 3 | F | 20160830 | 20151002 | 20160830 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-14141410 | BRISTOL MYERS SQUIBB | 45.00 | YR | F | Y | 0.00000 | 20160830 | OT | IT | IT |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 115879573 | 11587957 | 1 | PS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | UNK | Y | 9218 | |||||||||
| 115879573 | 11587957 | 2 | SS | ENOXAPARIN SODIUM. | ENOXAPARIN SODIUM | 1 | Subcutaneous | 1 DF, UNK | Y | 0 | 1 | DF | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 115879573 | 11587957 | 1 | Anticoagulant therapy |
| 115879573 | 11587957 | 2 | Anticoagulant therapy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 115879573 | 11587957 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 115879573 | 11587957 | Caesarean section | |
| 115879573 | 11587957 | International normalised ratio increased | |
| 115879573 | 11587957 | Live birth | |
| 115879573 | 11587957 | Maternal exposure during pregnancy | |
| 115879573 | 11587957 | Off label use |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |